Paediatric Haematology Research Unit
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- 1992
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Mark
Cholelithiasis during the first year of life : Case reports and literature review
(
- Contribution to journal › Article
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Mark
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden
(
- Contribution to journal › Article
-
Mark
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
(
- Contribution to journal › Article
-
Mark
Factor VIII and factor IX inhibitors in haemophiliacs
(
- Contribution to journal › Letter
-
Mark
Gaucher's disease in an infant diagnosed by fine needle aspiration of the liver and spleen : A case report
(
- Contribution to journal › Article
-
Mark
Haplotype analysis of identical factor IX mutants using PCR
(
- Contribution to journal › Article
-
Mark
Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A
(
- Contribution to journal › Letter
-
Mark
Implantable central venous catheter facilitates prophylactic treatment in children with haemophilia
(
- Contribution to journal › Article
-
Mark
Origin of mutation in sporadic cases of haemophilia-B
(
- Contribution to journal › Article
- 1991
-
Mark
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding